How to Read a Systematic Review and Meta

Clinical Review & Education
Users' Guides to the Medical Literature
How to Read a Systematic Review and Meta-analysis
and Apply the Results to Patient Care
Users’ Guides to the Medical Literature
Mohammad Hassan Murad, MD, MPH; Victor M. Montori, MD, MSc; John P. A. Ioannidis, MD, DSc;
Roman Jaeschke, MD, MSc; P. J. Devereaux, MD, PhD; Kameshwar Prasad, MD, DM, FRCPE;
Ignacio Neumann, MD, MSc; Alonso Carrasco-Labra, DDS, MSc; Thomas Agoritsas, MD; Rose Hatala, MD, MSc;
Maureen O. Meade, MD; Peter Wyer, MD; Deborah J. Cook, MD, MSc; Gordon Guyatt, MD, MSc
Clinical decisions should be based on the totality of the best evidence and not the results of
individual studies. When clinicians apply the results of a systematic review or meta-analysis to
patient care, they should start by evaluating the credibility of the methods of the systematic
review, ie, the extent to which these methods have likely protected against misleading
results. Credibility depends on whether the review addressed a sensible clinical question;
included an exhaustive literature search; demonstrated reproducibility of the selection and
assessment of studies; and presented results in a useful manner. For reviews that are
sufficiently credible, clinicians must decide on the degree of confidence in the estimates that
the evidence warrants (quality of evidence). Confidence depends on the risk of bias in the
body of evidence; the precision and consistency of the results; whether the results directly
apply to the patient of interest; and the likelihood of reporting bias. Shared decision making
requires understanding of the estimates of magnitude of beneficial and harmful effects, and
confidence in those estimates.
You are consulted regarding the perioperative management of a 66year-old man undergoing hip replacement. He is a smoker and has
a history of type 2 diabetes and hypertension. Because he has multiple cardiovascular risk factors, you consider using perioperative
β-blockers to reduce the risk of postoperative cardiovascular complications. You identify a recently published systematic review and
meta-analysis evaluating the effect of perioperative β-blockers on
death, nonfatal myocardial infarction, and stroke.1 How should you
use this meta-analysis to help guide your clinical decision making?
Introduction and Definitions
Traditional, unstructured review articles are useful for obtaining a
broad overview of a clinical condition but may not provide a reliable and unbiased answer to a focused clinical question. A systematic review is a research summary that addresses a focused clinical
question in a structured, reproducible manner. It is often, but not
always, accompanied by a meta-analysis, which is a statistical pooling or aggregation of results from different studies providing a single
estimate of effect. Box 1 summarizes the typical process of a systematic review and meta-analysis including the safeguards against
misleading results.
CME Quiz at
jamanetworkcme.com and
CME Questions page 186
Author Affiliations: Author
affiliations are listed at the end of this
article.
Corresponding Author: M. Hassan
Murad, MD, MPH, Mayo Clinic,
200 1st St, SW, Rochester, MN 55905
([email protected]).
JAMA. 2014;312(2):171-179. doi:10.1001/jama.2014.5559
Clinical Scenario
Supplemental content at
jama.com
In 1994, a Users’ Guide on how to use an “overview article”2 was
published in JAMA and presented a framework for critical appraisal
of systematic reviews. In retrospect, this framework did not distinguish between 2 very different issues: the rigor of the review methods and the confidence in estimates (quality of evidence) that the
results warrant. The current Users’ Guide reflects the evolution of
thinking since that time and presents a contemporary conceptualization.
We refer to the first judgment as the credibility3 of the review:
the extent to which its design and conduct are likely to have protected against misleading results.4 Credibility may be undermined
by inappropriate eligibility criteria, inadequate literature search, or
failure to optimally summarize results. A review with credible methods, however, may leave clinicians with low confidence in effect estimates. Therefore, the second judgment addresses the confidence in estimates.5 Common reasons for lower confidence include
high risk of bias of the individual studies; inconsistent results; and
small sample size of the body of evidence, leading to imprecise estimates. This Users’ Guide presents criteria for judging both credibility and confidence in the estimates (Box 2).
This guide focuses on a question of therapy and is intended for
clinicians applying the results to patient care. It does not provide comprehensive advice to researchers on how to conduct6 or report7 reviews. We also provide a rationale for seeking systematic reviews
and meta-analyses and explaining the summary estimate of a metaanalysis.
jama.com
JAMA July 9, 2014 Volume 312, Number 2
Copyright 2014 American Medical Association. All rights reserved.
Downloaded From: http://jama.jamanetwork.com/ by a Universidad de Chile User on 10/07/2014
171
Clinical Review & Education Users' Guides to the Medical Literature
Applying Systematic Review and Meta-analysis
Box 1. The Process of Conducting a Systematic Review
and Meta-analysis
Box 2. Guide for Appraising and Applying the Results
of a Systematic Review and Meta-analysisa
1. Formulate the question
2. Define the eligibility criteria for studies to be included in terms
of Patient, Intervention, Comparison, Outcome (PICO), and
study design
3. Develop a priori hypotheses to explain heterogeneity
4. Conduct search
5. Screen titles and abstracts for inclusion
6. Review full text of possibly eligible studies
7. Assess the risk of bias
8. Abstract data
9. When meta-analysis is performed:
• Generate summary estimates and confidence intervals
• Look for explanations of heterogeneity
• Rate confidence in estimates of effect
First Judgment: Evaluate the Credibility of the Methods
of Systematic Review
Did the review explicitly address a sensible clinical question?
Was the search for relevant studies exhaustive?
Were selection and assessments of studies reproducible?
Did the review present results that are ready for clinical application?
Did the review address confidence in estimates of effect?
Second Judgment: Rate the Confidence in the Effect Estimates
How serious is the risk of bias in the body of evidence?
Are the results consistent across studies?
How precise are the results?
Do the results directly apply to my patient?
Why Seek Systematic Reviews and Meta-analysis?
Is there concern about reporting bias?
When searching for evidence to answer a clinical question, it is preferable to seek a systematic review, especially one that includes a
meta-analysis. Single studies are liable to be unrepresentative of the
total evidence and be misleading.8 Collecting and appraising multiple studies require time and expertise that practitioners may not
have. Systematic reviews include a greater range of patients than
any single study, potentially enhancing confidence in applying the
results to the patient at hand.
Meta-analysis of a body of evidence includes a larger sample size
and more events than any individual study, leading to greater precision of estimates, facilitating confident decision making. Metaanalysis also provides an opportunity to explore reasons for inconsistency among studies.
A key limitation of systematic reviews and meta-analyses is that
they produce estimates that are as reliable as the studies summarized. A pooled estimate derived from meta-analysis of randomized trials at low risk of bias will always be more reliable than that
derived from a meta-analysis of observational studies or of randomized trials with less protection against bias.
Are there reasons to increase the confidence rating?
First Judgment: Was the Methodology
of the Systematic Review Credible?
Did the Review Explicitly Address a Sensible Clinical Question?
Systematic reviews of therapeutic questions should have a clear
focus and address questions defined by particular patients, interventions, comparisons, and outcomes (PICO). When a metaanalysis is conducted, the issue of how narrow or wide the scope
of the question becomes particularly important. Consider 4 hypothetical examples of meta-analyses with varying scope: (1) the
effect of all cancer treatments on mortality or disease progression; (2) the effect of chemotherapy on prostate cancer–specific
mortality; (3) the effect of docetaxel in castration-resistant prostate cancer on cancer-specific mortality; (4) the effect of
docetaxel in metastatic castration-resistant prostate cancer on
cancer-specific mortality
These 4 questions represent a gradually narrowing focus in
terms of patients, interventions, and outcomes. Clinicians will be uncomfortable with a meta-analysis of the first question and likely of
the second. Combining the results of these studies would yield an
estimate of effect that would make little sense or be misleading. Com172
a
Systematic reviews can address multiple questions. This guide is applied to
aspects of the systematic review that answer the clinical question at
hand—ideally the effect of the intervention vs the comparator of interest on
all outcomes of importance to patients.
fort level in combining studies increases in the third and fourth questions, although clinicians may even express concerns about the fourth
question because it combines symptomatic and asymptomatic populations.
What makes a meta-analysis too broad or too narrow? Clinicians need to decide whether, across the range of patients, interventions or exposures, and outcomes, it is plausible that the intervention will have a similar effect. This decision will reflect an
understanding of the underlying biology and may differ between individuals; it will only be possible, however, when systematic reviewers explicitly present their eligibility criteria.
Was the Search for Relevant Studies Exhaustive?
Systematic reviews are at risk of presenting misleading results if they
fail to secure a complete or representative sample of the available
eligible studies. For most clinical questions, searching a single database is insufficient. Searching MEDLINE, EMBASE, and the
Cochrane Central Register of Controlled Trials may be a minimal requirement for most clinical questions6 but for many questions will
not uncover all eligible articles. For instance, one study demonstrated that searching MEDLINE and EMBASE separately retrieved, respectively, only 55% and 49% of the eligible trials.9 Another study found that 42% of published meta-analyses included
at least 1 trial not indexed in MEDLINE.10 Multiple synonyms and
search terms to describe each concept are needed.
Additional references are identified through searching trial registries, bibliography of included studies, abstract presentations, contacting experts in the field, or searching databases of pharmaceutical companies and agencies such as the US Food and Drug
Administration.
Were Selection and Assessments of Studies Reproducible?
Systematic reviewers must decide which studies to include, the
extent of risk of bias, and what data to abstract. Although they
JAMA July 9, 2014 Volume 312, Number 2
Copyright 2014 American Medical Association. All rights reserved.
Downloaded From: http://jama.jamanetwork.com/ by a Universidad de Chile User on 10/07/2014
jama.com
Applying Systematic Review and Meta-analysis
follow an established protocol, some of their decisions will be
subjective and prone to error. Having 2 or more reviewers participate in each decision may reduce error and subjectivity. Systematic reviewers often report a measure of agreement on study
selection and quality appraisal (eg, κ statistic). If there is good
agreement between the reviewers, the clinician can have more
confidence in the process.
Did the Review Present Results That Are Ready
for Clinical Application?
Meta-analyses provide estimates of effect size (the magnitude of difference between groups).11 The type of effect size depends on the
nature of the outcome (relative risk, odds ratio, differences in risk,
hazard ratios, weighted mean difference, and standardized mean difference). Standardized effect sizes are expressed in multiples of the
standard deviation. This facilitates comparison of studies, irrespective of units of measure or the measurement scale.
Results of meta-analyses are usually depicted in a forest plot.
The point estimate of each study is typically presented as a square
with a size proportional to the weight of the study, and the confidence interval (CI) is presented as a horizontal line. The combined
summary effect, or pooled estimate, is typically presented as a diamond, with its width representing the confidence or credible interval (the CI indicates the range in which the true effect is likely to lie).
Forest plots for the perioperative β-blockers scenario are shown in
the Figure.
Meta-analysis provides a weighted average of the results of the
individual studies in which the weight of the study depends on its
precision. Studies that are more precise (ie, have narrower CIs) will
have greater weight and thus more influence on the combined estimate. For binary outcomes such as death, the precision depends
on the number of events and sample size. In panel B of the Figure,
the POISE trial12 had the largest number of deaths (226) and the largest sample size (8351); therefore, it had the narrowest CI and the largest weight (the effect from the trial is very similar to the combined
effect). Smaller trials with smaller numbers of events in that plot have
a much wider CI, and their effect size is quite different from the combined effect (ie, had less weight in meta-analysis). The weighting of
continuous outcomes is also based on the precision of the study,
which in this case depends on the sample size and SD (variability)
of each study.
In most meta-analyses such as the one in this clinical scenario,
aggregate data from each study are combined (ie, study-level data).
When data on every individual enrolled in each of the studies are
available, individual-patient data meta-analysis is conducted. This
approach facilitates more detailed analysis that can address issues
such as true intention-to-treat and subgroup analyses.
Relative association measures and continuous outcomes pose
challenges to risk communication and trading off benefits and harms.
Patients at high baseline risk can expect more benefit than those at
lower baseline risk from the same intervention (the same relative
effect). Meta-analysis authors can facilitate decision making by providing absolute effects in populations with various risk levels.13,14 For
example, given 2 individuals, one with low Framingham risk of cardiovascular events (2%) and the other with a high risk (28%), we can
multiply each of these baseline risks with the 25% relative risk reduction obtained from a meta-analysis of statin therapy trials.15 The
resulting absolute risk reduction (ie, risk difference) attributable to
Users' Guides to the Medical Literature Clinical Review & Education
statin therapy would be 0.5% for the low-risk individual and 7% for
the high-risk individual.
Continuous outcomes can also be presented in more useful
ways. Improvement of a dyspnea score by 1.06 scale points can be
better understood by informing readers that the minimal amount
considered by patients to be important on that scale is 0.5 points.16
A standardized effect size (eg, paroxetine reduced depression severity by 0.31 SD units) can be better understood if (1) referenced
to cutoffs of 0.2, 0.5, and 0.8 that represent small, moderate, and
large effect, respectively; (2) translated back to natural units with
which clinicians have more familiarity (eg, converted to a change of
2.47 on the Hamilton Rating Scale for Depression); or (3) dichotomized (for every 100 patients treated with paroxetine, 11 will achieve
important improvement).17
Did the Review Address Confidence in Estimates of Effect?
A well-conducted (ie, credible) systematic review should present
readers with information needed to make their second judgement:
the confidence in the effect estimates. For example, if systematic
reviewers do not evaluate the risk of bias in the individual studies
or attempt to explain heterogeneity, this second judgement will not
be possible.
In Box 3, we return to the clinical scenario to determine credibility of the systematic review identified. Overall, you conclude that
the credibility of the methods of this systematic review is high and
move on to examine the estimates of effect and the associated confidence in these estimates.
Second Judgment: What Is the Confidence in the Estimates
of Effect?
Several systems are used to evaluate the quality of evidence, of which
4 are most commonly used: the Grading of Recommendations Assessment, Development and Evaluation (GRADE) and the systems
from the American Heart Association, the US Preventive Services
Task Force, and the Oxford Centre for Evidence-Based
Medicine.5,18-20 These systems share the similar features of being
used by multiple organizations and providing a confidence rating in
the estimates that gives randomized trials a higher rating than nonrandomized studies. The 4 systems are described in eTable 1 in the
Supplement.
The general framework used in this Users’ Guide follows the
GRADE approach.21 GRADE categorizes confidence in 4 categories: high, moderate, low, or very low. The lower the confidence,
the more likely the underlying true effect is substantially different
from the observed estimate of effect and, thus, the more likely
that further research would demonstrate different estimates.5
Confidence ratings begin by considering study design. Randomized trials are initially assigned high confidence and observational
studies are given low confidence, but a number of factors may modify
these initial ratings. Confidence may decrease when there is high risk
of bias, inconsistency, imprecision, indirectness, or concern about
publication bias. An increase in confidence rating is uncommon and
occurs primarily in observational studies when the effect size is large.
Readers of a systematic review can consider these factors regardless of whether systematic review authors formally used this approach. Readers do, however, require the necessary information, and
thus the need for a final credibility guide: Did the Review Address
Confidence in Estimates of Effect?
jama.com
JAMA July 9, 2014 Volume 312, Number 2
Copyright 2014 American Medical Association. All rights reserved.
Downloaded From: http://jama.jamanetwork.com/ by a Universidad de Chile User on 10/07/2014
173
Clinical Review & Education Users' Guides to the Medical Literature
Applying Systematic Review and Meta-analysis
Figure. Results of a Meta-analysis of the Outcomes of Nonfatal Infarction, Death, and Nonfatal Stroke in
Patients Receiving Perioperative β-Blockers
A Nonfatal myocardial infarction
β-Blockers
Total,
Events, No.
No.
Source
Low risk of bias
DIPOM
3
MaVS
19
POISE
152
POBBLE
3
BBSA
1
Subtotal (I 2 = 0%; P = .70)
462
246
4174
55
110
High risk of bias
Poldermans
0
59
Dunkelgrun
11
533
Subtotal (I 2 = 57%; P = .13)
Overall
I 2 = 29%; P = .21
Interaction test between groups, P = .22
B
Control
Total,
No.
2
21
215
5
0
459
250
4177
48
109
1.49 (0.25-8.88)
0.92 (0.51-1.67)
0.71 (0.58-0.87)
0.52 (0.13-2.08)
2.97 (0.12-72.19)
0.73 (0.61-0.88)
9
27
53
533
0.05 (0.00-0.79)
0.41 (0.20-0.81)
0.21 (0.03-1.61)
0.67 (0.47-0.96)
RR
(95% CI)
0.01
0.1
Favors
Control
1.0
10
100
Risk Ratio (95% CI)
Death
β-Blockers
Events,
Total,
No.
No.
Source
Low risk of bias
BBSA
1
Bayliff
2
DIPOM
20
MaVS
0
Neary
3
POISE
129
Mangano
4
POBBLE
3
Yang
0
Subtotal (I 2 = 0%; P = .68)
High risk of bias
Poldermans
2
Dunkelgrun
10
Subtotal (I 2 = 44%; P = .18)
Overall
Control
Favors
β-Blockers
Events, No.
Total,
No.
110
49
462
246
18
4174
99
55
51
0
1
15
4
5
97
5
1
1
109
50
459
250
20
4177
101
48
51
2.97 (0.12-72.19)
2.04 (0.19-21.79)
1.32 (0.69-2.55)
0.11 (0.01-2.09)
0.67 (0.19-2.40)
1.33 (1.03-1.73)
0.82 (0.23-2.95)
2.62 (0.28-24.34)
0.33 (0.01-8.00)
1.27 (1.01-1.60)
59
533
9
16
53
533
0.20 (0.05-0.88)
0.63 (0.29-1.36)
0.42 (0.15-1.23)
0.94 (0.63-1.40)
RR
(95% CI)
I 2 = 30%; P = .16
Interaction test between groups, P = .04
C
Favors
β-Blockers
Events, No.
0.01
0.1
Favors
Control
1.0
10
100
Risk Ratio (95% CI)
Nonfatal stroke
β-Blockers
Events,
Total,
No.
No.
Source
Low risk of bias
POBBLE
1
DIPOM
2
MaVS
5
Yang
0
POISE
27
Subtotal (I 2 = 0%; P = .60)
53
462
246
51
4174
Control
Events,
Total,
No.
No.
0
0
4
2
14
44
459
250
51
4177
3
533
High risk of bias
Dunkelgrun
4
533
Overall
I 2 = 0%; P = .71
Interaction test between groups, P = .75
Favors
β-Blockers
RR
(95% CI)
Favors
Control
2.50 (0.10-59.88)
4.97 (0.24-103.19)
1.27 (0.35-4.67)
0.20 (0.01-4.07)
1.93 (1.01-3.68)
1.73 (1.00-2.99)
1.33 (0.30-5.93)
1.67 (1.00-2.80)
0.01
0.1
1.0
10
100
Risk Ratio (95% CI)
How Serious Is the Risk of Bias in the Body of Evidence?
A well-conducted systematic review should always provide readers with insight about the risk of bias in each individual study
and overall.6,7 Differences in studies’ risk of bias can explain impor174
Abbreviations: BBSA, Beta Blocker in
Spinal Anesthesia study; DIPOM,
Diabetic Postoperative Mortality and
Morbidity trial; MaVS, Metoprolol
after Vascular Surgery study;
POBBLE, Perioperative β-blockade
trial; POISE, Perioperative Ischemic
Evaluation trial. Dotted line indicates
no effect. Dashed line is centered on
meta-analysis pooled estimate.
tant differences in results.22 Less rigorous studies sometimes
overestimate the effectiveness of therapeutic and preventive
interventions.23 The effects of antioxidants on the risk of prostate
cancer24 and on atherosclerotic plaque formation25 are 2 of many
JAMA July 9, 2014 Volume 312, Number 2
Copyright 2014 American Medical Association. All rights reserved.
Downloaded From: http://jama.jamanetwork.com/ by a Universidad de Chile User on 10/07/2014
jama.com
Clinical Review & Education
Users' Guides to the Medical Literature
How to Read a Systematic Review and Meta-analysis
and Apply the Results to Patient Care
Users’ Guides to the Medical Literature
Mohammad Hassan Murad, MD, MPH; Victor M. Montori, MD, MSc; John P. A. Ioannidis, MD, DSc;
Roman Jaeschke, MD, MSc; P. J. Devereaux, MD, PhD; Kameshwar Prasad, MD, DM, FRCPE;
Ignacio Neumann, MD, MSc; Alonso Carrasco-Labra, DDS, MSc; Thomas Agoritsas, MD; Rose Hatala, MD, MSc;
Maureen O. Meade, MD; Peter Wyer, MD; Deborah J. Cook, MD, MSc; Gordon Guyatt, MD, MSc
Clinical decisions should be based on the totality of the best evidence and not the results of
individual studies. When clinicians apply the results of a systematic review or meta-analysis to
patient care, they should start by evaluating the credibility of the methods of the systematic
review, ie, the extent to which these methods have likely protected against misleading
results. Credibility depends on whether the review addressed a sensible clinical question;
included an exhaustive literature search; demonstrated reproducibility of the selection and
assessment of studies; and presented results in a useful manner. For reviews that are
sufficiently credible, clinicians must decide on the degree of confidence in the estimates that
the evidence warrants (quality of evidence). Confidence depends on the risk of bias in the
body of evidence; the precision and consistency of the results; whether the results directly
apply to the patient of interest; and the likelihood of reporting bias. Shared decision making
requires understanding of the estimates of magnitude of beneficial and harmful effects, and
confidence in those estimates.
You are consulted regarding the perioperative management of a 66year-old man undergoing hip replacement. He is a smoker and has
a history of type 2 diabetes and hypertension. Because he has multiple cardiovascular risk factors, you consider using perioperative
β-blockers to reduce the risk of postoperative cardiovascular complications. You identify a recently published systematic review and
meta-analysis evaluating the effect of perioperative β-blockers on
death, nonfatal myocardial infarction, and stroke.1 How should you
use this meta-analysis to help guide your clinical decision making?
Introduction and Definitions
Traditional, unstructured review articles are useful for obtaining a
broad overview of a clinical condition but may not provide a reliable and unbiased answer to a focused clinical question. A systematic review is a research summary that addresses a focused clinical
question in a structured, reproducible manner. It is often, but not
always, accompanied by a meta-analysis, which is a statistical pooling or aggregation of results from different studies providing a single
estimate of effect. Box 1 summarizes the typical process of a systematic review and meta-analysis including the safeguards against
misleading results.
CME Quiz at
jamanetworkcme.com and
CME Questions page 186
Author Affiliations: Author
affiliations are listed at the end of this
article.
Corresponding Author: M. Hassan
Murad, MD, MPH, Mayo Clinic,
200 1st St, SW, Rochester, MN 55905
([email protected]).
JAMA. 2014;312(2):171-179. doi:10.1001/jama.2014.5559
Clinical Scenario
Supplemental content at
jama.com
In 1994, a Users’ Guide on how to use an “overview article”2 was
published in JAMA and presented a framework for critical appraisal
of systematic reviews. In retrospect, this framework did not distinguish between 2 very different issues: the rigor of the review methods and the confidence in estimates (quality of evidence) that the
results warrant. The current Users’ Guide reflects the evolution of
thinking since that time and presents a contemporary conceptualization.
We refer to the first judgment as the credibility3 of the review:
the extent to which its design and conduct are likely to have protected against misleading results.4 Credibility may be undermined
by inappropriate eligibility criteria, inadequate literature search, or
failure to optimally summarize results. A review with credible methods, however, may leave clinicians with low confidence in effect estimates. Therefore, the second judgment addresses the confidence in estimates.5 Common reasons for lower confidence include
high risk of bias of the individual studies; inconsistent results; and
small sample size of the body of evidence, leading to imprecise estimates. This Users’ Guide presents criteria for judging both credibility and confidence in the estimates (Box 2).
This guide focuses on a question of therapy and is intended for
clinicians applying the results to patient care. It does not provide comprehensive advice to researchers on how to conduct6 or report7 reviews. We also provide a rationale for seeking systematic reviews
and meta-analyses and explaining the summary estimate of a metaanalysis.
jama.com
JAMA July 9, 2014 Volume 312, Number 2
Copyright 2014 American Medical Association. All rights reserved.
Downloaded From: http://jama.jamanetwork.com/ by a Universidad de Chile User on 10/07/2014
171
Clinical Review & Education Users' Guides to the Medical Literature
Applying Systematic Review and Meta-analysis
Box 4. Using the Guide: Judgment 2, Determining the Confidence in the Estimates (Perioperative β-Blockers in Noncardiac Surgery)1
See the Table for the raw data used in this discussion.
How to Calculate Risk Difference (Absolute Risk Reduction
or Increase)?
In the Figure, the risk ratio (RR) for nonfatal myocardial infarction is
0.73. The baseline risk (risk without perioperative β-blockers) can be
obtained from the trial that is the largest and likely enrolled most representative population12 (215/4177, approximately 52 per 1000). The
risk with intervention would be (52/1000 × 0.73, approximately 38
per 1000). The absolute risk difference would be (52/1000 − 38/
1000 = −14, approximately 14 fewer myocardial infarctions per 1000).
The same process can be used to calculate the confidence intervals
around the risk difference, substituting the boundaries of the confidence interval (CI) of the RR for the point estimate.
The number needed to treat to prevent 1 nonfatal myocardial infarction can also be calculated as the inverse of the absolute risk difference (1/0.014 = 72 patients).
Risk of Bias
Of the 11 trials included in the analysis, 2 were considered to have high
risk of bias.35,36 Limitations included lack of blinding, stopping early because of large apparent benefit,36 and concerns about the integrity of
the data.1 The remaining 9 trials had adequate bias protection measures
and represented a body of evidence that was at low risk of bias.
Inconsistency
Visual inspection of forest plots (Figure) shows that the point estimates, for both nonfatal myocardial infarction and death, substantially differ across studies. For the outcome of stroke, results are extremely consistent. There is minimal overlap of CIs of point estimates
for the analysis of death. Confidence intervals in the analysis of nonfatal myocardial infarction do overlap to a great extent and fully overlap in the outcome of stroke. Heterogeneity P values were .21 for nonfatal myocardial infarction, .16 for death, and .71 for stroke; I2 values
were 29%, 30%, and 0%, respectively. A test of interaction between the 2 groups of studies (high risk of bias vs low risk of bias) yields
a nonsignificant P value of .22 for myocardial infarction (suggesting
that the difference between these 2 subgroups of studies could be
attributable to chance) and a significant P value of .04 for the outcome of death. Considering that the observed heterogeneity is at least
partially explained by the risk of bias and that the trials with low risk
of bias for all outcomes are consistent, you decide to obtain the estimates of effect from the trials with low risk of bias and do not lower
the confidence rating because of inconsistency.
Imprecision
For the outcomes of death and nonfatal stroke, clinical decisions would
differ if the upper vs the lower boundaries of the CI represented the
truth; therefore, imprecision makes us lose confidence in both estimates. No need to lower the confidence rating for nonfatal myocardial infarction.
Indirectness
The age of the majority of patients enrolled across the trials ranged
between 50 and 70, similar to the patient in the opening scenario,
who is 66 years old. Most of the trials enrolled patients with risk factors for heart disease undergoing surgical procedures classified as intermediate surgical risk, similar to the risk factors and hip surgery of
the patient. Although the drug used and the dose varied across trials,
the consistent results suggest we can use a modest dose of the
β-blocker with which we are most familiar. The outcomes of death,
nonfatal stroke, and nonfatal infarction are the key outcomes of importance to patients. Overall, the available evidence presented in the
systematic review is direct and applicable to the patient of interest
and addresses the key outcomes.
Reporting Bias
The authors of the systematic review and meta-analysis constructed funnel plots that appear to be symmetrical and results of the
statistical tests for the symmetry of the plot were nonsignificant, leaving no reason for lowering the confidence rating because of possible
reporting or publication bias.
Confidence in the Estimates
Overall, evidence warranting high confidence suggests that individuals with risk factors for heart disease can expect a reduction in
risk of a perioperative nonfatal infarction of 14 in 1000 (from
approximately 20 per 1000 to 6 per 1000). Unfortunately, they
can also expect an increase in their risk of dying or having a nonfatal stroke. Because most people are highly averse to stroke and
death, it is likely that the majority of patients faced with this evidence would decline β-blockers as part of their perioperative regimen. Indeed, that is what this patient decides when informed
about the evidence.
Table. Evidence Summary of the Perioperative β-Blockers Question
Outcome
No. of
Participants
(Trials)
Confidence
Relative Effect (95% CI)
Risk Difference per 1000
Patientsa
14 fewer (6 fewer to 20 fewer)
Nonfatal myocardial
infarction
10 189 (5)
High
0.73 (0.61-0.88)
Stroke
10 186 (5)
Moderate
1.73 (1.00- 2.99)
2 more (0 more to 6 more)
Death
10 529 (9)
Moderate
1.27 (1.01-1.60)
6 more (0 more to 13 more)
their patients were the upper boundary to represent the truth and
how they would advise their patients were the lower boundary to
represent the truth. If the advice would be the same in either case,
then the evidence is sufficiently precise. If decisions would change
across the range of the confidence interval, then confidence in the
evidence will decrease.34
176
a
See Box 4.
For instance, consider the results of nonfatal myocardial infarction in the β-blocker example (Box 4 and Table). The CI around the
absolute effect of β-blockers is a reduction of from 6 (the minimum) to 20 (the maximum) infarctions in 1000 patients given
β-blockers. Considering this range of plausible effects, clinicians must
ask themselves: Would my patients make different choices about
JAMA July 9, 2014 Volume 312, Number 2
Copyright 2014 American Medical Association. All rights reserved.
Downloaded From: http://jama.jamanetwork.com/ by a Universidad de Chile User on 10/07/2014
jama.com
Applying Systematic Review and Meta-analysis
the use of β-blockers if their risk of infarction decreased by only 6
in 1000 or by as much as 20 in 1000?
One might readily point out that this judgment is subjective—it
is a matter of values and preferences. Quite so, but that is the nature of clinical decision making: the trade-off between the desirable and undesirable consequences of the alternative courses of action is a matter of values and preferences and is therefore subjective.
To the extent that clinicians are confident that patients would place
similar weight on reductions of 6 and 20 in 1000 infarctions, concern about imprecision will be minimal. To the extent that clinicians
are confident that patients will view 6 in 1000 as trivial and 20 in
1000 as important, concern about imprecision will be large. To the
extent that clinicians are uncertain of their patients’ values and preferences on the matter, judgments about imprecision will be similarly insecure.
The judgment regarding myocardial infarction may leave clinicians with doubt about imprecision—much less so for stroke and
death (Box 4 and Table). With regard to both, if the boundary most
favoring β-blockers (ie, no increase in death and stroke) represented the truth, patients would have no reluctance regarding use
of β-blockers. On the other hand, if risk of death and stroke increased by, respectively, 13 and 6, reluctance regarding use of
β-blockers would increase substantially. Given uncertainty about
which extreme represents the truth, confidence in estimates decreases because of imprecision.
Do the Results Directly Apply to My Patient?
The optimal evidence for decision making comes from research that
directly compared the interventions in which we are interested,
evaluated in the populations in which we are interested, and measured outcomes important to patients. If populations, interventions, or outcomes in studies differ from those of interest, the evidence can be viewed as indirect.
A common example of indirectness of population is when we
treat a very elderly patient using evidence derived from trials that
excluded elderly persons. Indirectness of outcomes occurs when
trials use surrogate end points (eg, hemoglobin A1c level), whereas
patients are most concerned about other outcomes (eg, macrovascular and microvascular disease).37 Indirectness also occurs when
clinicians must choose between interventions that have not been
tested in head-to-head comparisons.38 For instance, many trials have
compared osteoporosis drugs with placebo, but very few have compared them directly against one another.39 Making comparisons between treatments under these circumstances requires extrapolation from existing comparisons and multiple assumptions.40
Decisions regarding indirectness of patients and interventions
depend on an understanding of whether biologic or social factors
are sufficiently different that one might expect substantial differences in the magnitude of effect. Indirectness can lead to lowering
confidence in the estimates.38
Is There Concern About Reporting Bias?
When researchers base their decision to publish certain material on
the magnitude, direction, or statistical significance of the results, a
systematic error called reporting bias occurs. This is the most difficult type of bias to address in systematic reviews. When an entire
study remains unreported, the standard term is publication bias. It
has been shown that the magnitude and direction of results may be
Users' Guides to the Medical Literature Clinical Review & Education
more important determinants of publication than study design, relevance, or quality41 and that positive studies may be as much as 3
times more likely to be published than negative studies.42 When authors or study sponsors selectively report specific outcomes or analyses, the term selective outcome reporting bias is used.43
Empirical evidence suggests that half of the analysis plans of randomized trials are different in protocols than in published reports.44
Reporting bias can create misleading estimates of effect. A study of
the US Food and Drug Administration reports showed that they often included numerous unpublished studies and that the findings
of these studies can alter the estimates of effect.45 Data on 74% of
patients enrolled in the trials evaluating the antidepressant reboxetine were unpublished. Published data overestimated the benefit
of reboxetine vs placebo by 115% and vs other antidepressants by
23%, and also underestimated harm.46
Detecting publication bias in a systematic review is difficult.
When it includes a meta-analysis, a common approach is to examine whether the results of small studies differ from those of larger
ones. In a figure that relates the precision (as measured by sample
size, SE, or variance) of studies included in a meta-analysis to the
magnitude of treatment effect, the resulting display should resemble an inverted funnel (eFigure, panel A in the Supplement). Such
funnel plots should be symmetric around the combined effect. A gap
or empty area in the funnel suggests that studies may have been conducted and not published (eFigure, panel B in the Supplement).
Other explanations for asymmetry are, however, possible. Small studies may have a higher risk of bias explaining their larger effects, may
have enrolled a more responsive patient group, or may have administered the intervention more meticulously. Last, there is always the
possibility of a chance finding.
Several empirical tests have been developed to detect publication bias. Unfortunately, all have serious limitations, require a large
number of studies (ideally 30 or more),47 and none has been validated against a criterion standard of real data in which we know
whether bias existed.47
More compelling than any of these theoretical exercises is the
success of systematic reviewers in obtaining the results of unpublished studies. Prospective study registration with accessible results may be a solution to reporting bias.48,49 Until complete reporting becomes a reality,50 clinicians using research reports to guide
their practice must remain cognizant of the dangers of reporting biases and, when they suspect bias, should lower their confidence in
the estimates.51
Are There Reasons to Increase the Confidence Rating?
Some uncommon situations warrant an increase in the confidence rating of effect estimates from observational studies. Consider our confidence in the effect of hip replacement on reducing pain and functional limitations in severe osteoarthritis, epinephrine to prevent
mortality in anaphylaxis, insulin to prevent mortality in diabetic
ketoacidosis, or dialysis to prolong life in patients with end-stage renal failure.52 In each of these situations, we observe a large treatment
effect achieved over a short period among patients with a condition
that would have inevitably worsened in the absence of an intervention. This large effect can increase confidence in a true association.52
Box 4 and the Table summarize the effect of β-blockers in patients undergoing noncardiac surgery and addresses our confidence in the apparent effects of the intervention.
jama.com
JAMA July 9, 2014 Volume 312, Number 2
Copyright 2014 American Medical Association. All rights reserved.
Downloaded From: http://jama.jamanetwork.com/ by a Universidad de Chile User on 10/07/2014
177
Clinical Review & Education Users' Guides to the Medical Literature
Conclusions
Clinical and policy decisions should be based on the totality of the best
evidence and not the results of individual studies. Systematic summa-
Applying Systematic Review and Meta-analysis
ries of the best available evidence are required for optimal clinical decision making. Applying the results of a systematic review and metaanalysis includes a first step in which we judge the credibility of the
methods of the systematic review and a second step in which we decide how much confidence we have in the estimates of effect.
ARTICLE INFORMATION
REFERENCES
Author Affiliations: Division of Preventive
Medicine and Knowledge and Evaluation Research
Unit, Mayo Clinic, Minnesota (Murad); Knowledge
and Evaluation Research Unit, Mayo Clinic,
Rochester, Minnesota (Montori); Departments of
Medicine and Health Research and Policy, Stanford
University School of Medicine; Department of
Statistics, Stanford University School of Humanities
and Sciences; and Meta-Research Innovation
Center at Stanford (METRICS), Stanford University,
Stanford, California (Ioannidis); Departments of
Medicine and Clinical Epidemiology and
Biostatistics, McMaster University, Hamilton,
Ontario, Canada (Jaeschke); Departments of
Medicine and Clinical Epidemiology and
Biostatistics and Population Health Research
Institute, McMaster University, Hamilton, Ontario,
Canada (Devereaux); All India Institute of Medical
Sciences, New Delhi (Prasad); Department of
Internal Medicine, School of Medicine, Pontificia
Universidad Católica de Chile, Santiago, Chile
(Neumann); Evidence-Based Dentistry Unit, Faculty
of Dentistry, Universidad de Chile, Santiago, Chile,
and Department of Clinical Epidemiology and
Biostatistics, McMaster University, Hamilton,
Ontario, Canada (Carrasco-Labra); Department
Clinical Epidemiology and Biostatistics, McMaster
University, Hamilton, Ontario, Canada (Agoritsas);
Department of Medicine, University of British
Columbia, Vancouver, British Columbia, Canada
(Hatala); Department of Clinical Epidemiology and
Biostatistics, McMaster University, Hamilton,
Ontario, Canada (Meade); Columbia University
Medical Center, New York, New York (Wyer);
Departments of Medicine and Clinical Epidemiology
and Biostatistics and Population Health Research
Institute, McMaster University, Hamilton, Ontario,
Canada (Cook); Departments of Medicine and
Clinical Epidemiology and Biostatistics, McMaster
University, Hamilton, Ontario, Canada (Guyatt).
1. Bouri S, Shun-Shin MJ, Cole GD, Mayet J, Francis
DP. Meta-analysis of secure randomised controlled
trials of β-blockade to prevent perioperative death
in non-cardiac surgery. Heart. 2014;100(6):456-464.
Author Contributions: Dr Murad had full access to
all of the data in the study and takes responsibility
for the integrity of the data and the accuracy of the
data analysis.
Conflict of Interest Disclosures: All authors have
completed and submitted the ICMJE Form for
Disclosure of Potential Conflicts of Interest. Drs
Murad and Montori receive funding from several
non-for-profit organizations to conduct systematic
reviews and meta-analysis. The Meta-Research
Innovation Center at Stanford (METRICS), directed
by Dr Ioannidis, is funded by a grant from the Laura
and John Arnold Foundation. Dr Agoritsas was
financially supported by Fellowship for Prospective
Researchers Grant No. PBGEP3-142251 from the
Swiss National Science Foundation. Dr Cook is a
Research Chair of the Canadian Institutes of Health
Research.
Disclaimer: Drs Murad, Montori, Jaeschke, Prasad,
Carrasco-Labra, Neumann, Agoritsas, and Guyatt
are members of the GRADE Working Group.
2. Oxman AD, Cook DJ, Guyatt GH; Evidence-Based
Medicine Working Group. Users’ guides to the
medical literature, VI: how to use an overview. JAMA.
1994;272(17):1367-1371.
3. Alkin M. Evaluation Roots: Tracing Theorists’
Views and Influences. Thousand Oaks, California: Sage
Publications Inc; 2004.
4. Oxman AD. Checklists for review articles. BMJ.
1994;309(6955):648-651.
5. Balshem H, Helfand M, Schünemann HJ, et al.
GRADE guidelines, 3: rating the quality of evidence.
J Clin Epidemiol. 2011;64(4):401-406.
6. Cochrane Handbook for Systematic Reviews of
Interventions. Version 5.1.0 ed. Chichester, United
Kingdom: John Wiley & Sons Ltd; 2011.
7. Moher D, Liberati A, Tetzlaff J, Altman DG;
PRISMA Group. Preferred reporting items for
systematic reviews and meta-analyses: the PRISMA
statement. J Clin Epidemiol. 2009;62(10):1006-1012.
8. Murad MH, Montori VM. Synthesizing evidence:
shifting the focus from individual studies to the
body of evidence. JAMA. 2013;309(21):2217-2218.
9. Hopewell S, Clarke M, Lefebvre C, Scherer R.
Handsearching versus electronic searching to
identify reports of randomized trials. Cochrane
Database Syst Rev. 2007;(2):MR000001.
10. Egger M, Juni P, Bartlett C, Holenstein F, Sterne
J. How important are comprehensive literature
searches and the assessment of trial quality in
systematic reviews? empirical study. Health Technol
Assess. 2003;7(1):1-76.
11. Livingston EH, Elliot A, Hynan L, Cao J. Effect
size estimation: a necessary component of
statistical analysis. Arch Surg. 2009;144(8):706-712.
12. Devereaux PJ, Yang H, Yusuf S, et al; POISE
Study Group. Effects of extended-release
metoprolol succinate in patients undergoing
non-cardiac surgery (POISE trial): a randomised
controlled trial. Lancet. 2008;371(9627):1839-1847.
13. Murad MH, Montori VM, Walter SD, Guyatt GH.
Estimating risk difference from relative association
measures in meta-analysis can infrequently pose
interpretational challenges. J Clin Epidemiol. 2009;
62(8):865-867.
14. Guyatt GH, Eikelboom JW, Gould MK, et al;
American College of Chest Physicians. Approach to
outcome measurement in the prevention of
thrombosis in surgical and medical patients:
Antithrombotic Therapy and Prevention of
Thrombosis, 9th ed: American College of Chest
Physicians Evidence-Based Clinical Practice
Guidelines. Chest. 2012;141(2)(suppl):e185S-e194S.
15. Taylor F, Huffman MD, Macedo AF, et al. Statins
for the primary prevention of cardiovascular
disease. Cochrane Database Syst Rev. 2013;1:
CD004816.
16. Lacasse Y, Martin S, Lasserson TJ, Goldstein RS.
Meta-analysis of respiratory rehabilitation in
chronic obstructive pulmonary disease: a Cochrane
systematic review. Eura Medicophys. 2007;43(4):
475-485.
17. Johnston BC, Patrick DL, Thorlund K, et al.
Patient-reported outcomes in meta-analyses-part
2: methods for improving interpretability for
decision-makers. Health Qual Life Outcomes. 2013;
11:211.
18. US Preventive Services Task Force (USPSTF).
Grade Definitions. USPSTF website. http://www
.uspreventiveservicestaskforce.org/uspstf/grades
.htm. Accessed May 23, 2014.
19. Jacobs AK, Kushner FG, Ettinger SM, et al.
ACCF/AHA clinical practice guideline methodology
summit report: a report of the American College of
Cardiology Foundation/American Heart Association
Task Force on Practice Guidelines. Circulation. 2013;
127(2):268-310.
20. Oxford Centre for Evidence-based Medicine
(OECBM) Levels of Evidence Working Group.
OECBM 2011 Levels of Evidence. OECBM website.
http://www.cebm.net/mod_product/design/files
/CEBM-Levels-of-Evidence-2.1.pdf. 2011. Accessed
May 25, 2014.
21. Guyatt GH, Oxman AD, Vist GE, et al; GRADE
Working Group. GRADE: an emerging consensus on
rating quality of evidence and strength of
recommendations. BMJ. 2008;336(7650):924-926.
22. Moher D, Pham B, Jones A, et al. Does quality
of reports of randomised trials affect estimates of
intervention efficacy reported in meta-analyses?
Lancet. 1998;352(9128):609-613.
23. Odgaard-Jensen J, Vist GE, Timmer A, et al.
Randomisation to protect against selection bias in
healthcare trials. Cochrane Database Syst Rev. 2011;
(4):MR000012.
24. Klein EA, Thompson IM Jr, Tangen CM, et al.
Vitamin E and the risk of prostate cancer: the
Selenium and Vitamin E Cancer Prevention Trial
(SELECT). JAMA. 2011;306(14):1549-1556.
25. Sesso HD, Buring JE, Christen WG, et al.
Vitamins E and C in the prevention of
cardiovascular disease in men: the Physicians’
Health Study II randomized controlled trial. JAMA.
2008;300(18):2123-2133.
26. Jüni P, Witschi A, Bloch R, Egger M. The
hazards of scoring the quality of clinical trials for
meta-analysis. JAMA. 1999;282(11):1054-1060.
27. Higgins JP, Altman DG, Gøtzsche PC, et al;
Cochrane Bias Methods Group; Cochrane Statistical
Methods Group. The Cochrane Collaboration’s tool
for assessing risk of bias in randomised trials. BMJ.
2011;343:d5928.
28. Hatala R, Keitz S, Wyer P, Guyatt G;
Evidence-Based Medicine Teaching Tips Working
178
JAMA July 9, 2014 Volume 312, Number 2
Copyright 2014 American Medical Association. All rights reserved.
Downloaded From: http://jama.jamanetwork.com/ by a Universidad de Chile User on 10/07/2014
jama.com
Applying Systematic Review and Meta-analysis
Group. Tips for learners of evidence-based
medicine, 4: assessing heterogeneity of primary
studies in systematic reviews and whether to
combine their results. CMAJ. 2005;172(5):661-665.
29. Lau J, Ioannidis JP, Schmid CH. Quantitative
synthesis in systematic reviews. Ann Intern Med.
1997;127(9):820-826.
30. Higgins JP, Thompson SG, Deeks JJ, Altman
DG. Measuring inconsistency in meta-analyses. BMJ.
2003;327(7414):557-560.
31. Altman DG, Bland JM. Interaction revisited: the
difference between two estimates. BMJ. 2003;
326(7382):219.
32. Navarese EP, Kowalewski M, Andreotti F, et al.
Meta-analysis of time-related benefits of statin
therapy in patients with acute coronary syndrome
undergoing percutaneous coronary intervention.
Am J Cardiol. 2014;113(10):1753-1764.
33. Guyatt GH, Oxman AD, Kunz R, et al; GRADE
Working Group. GRADE guidelines, 7: rating the
quality of evidence—inconsistency. J Clin Epidemiol.
2011;64(12):1294-1302.
34. Guyatt GH, Oxman AD, Kunz R, et al. GRADE
guidelines, 6: rating the quality of
evidence—imprecision. J Clin Epidemiol. 2011;64
(12):1283-1293.
35. Dunkelgrun M, Boersma E, Schouten O, et al;
Dutch Echocardiographic Cardiac Risk Evaluation
Applying Stress Echocardiography Study Group.
Bisoprolol and fluvastatin for the reduction of
perioperative cardiac mortality and myocardial
infarction in intermediate-risk patients undergoing
noncardiovascular surgery: a randomized
controlled trial (DECREASE-IV). Ann Surg. 2009;
249(6):921-926.
36. Poldermans D, Boersma E, Bax JJ, et al; Dutch
Echocardiographic Cardiac Risk Evaluation Applying
Users' Guides to the Medical Literature Clinical Review & Education
Stress Echocardiography Study Group. The effect of
bisoprolol on perioperative mortality and
myocardial infarction in high-risk patients
undergoing vascular surgery. N Engl J Med. 1999;
341(24):1789-1794.
37. Murad MH, Shah ND, Van Houten HK, et al.
Individuals with diabetes preferred that future trials
use patient-important outcomes and provide
pragmatic inferences. J Clin Epidemiol. 2011;64(7):
743-748.
38. Guyatt GH, Oxman AD, Kunz R, et al; GRADE
Working Group. GRADE guidelines, 8: rating the
quality of evidence—indirectness. J Clin Epidemiol.
2011;64(12):1303-1310.
39. Murad MH, Drake MT, Mullan RJ, et al.
Comparative effectiveness of drug treatments to
prevent fragility fractures: a systematic review and
network meta-analysis. J Clin Endocrinol Metab.
2012;97(6):1871-1880.
40. Mills EJ, Ioannidis JP, Thorlund K, Schünemann
HJ, Puhan MA, Guyatt GH. How to use an article
reporting a multiple treatment comparison
meta-analysis. JAMA. 2012;308(12):1246-1253.
randomized controlled trials: meta-epidemiologic
study. BMJ. 2013;347:f4313.
45. McDonagh MS, Peterson K, Balshem H,
Helfand M. US Food and Drug Administration
documents can provide unpublished evidence
relevant to systematic reviews. J Clin Epidemiol.
2013;66(10):1071-1081.
46. Eyding D, Lelgemann M, Grouven U, et al.
Reboxetine for acute treatment of major
depression: systematic review and meta-analysis of
published and unpublished placebo and selective
serotonin reuptake inhibitor controlled trials. BMJ.
2010;341:c4737.
47. Lau J, Ioannidis JP, Terrin N, Schmid CH, Olkin I.
The case of the misleading funnel plot. BMJ. 2006;
333(7568):597-600.
48. Boissel JP, Haugh MC. Clinical trial registries
and ethics review boards: the results of a survey by
the FICHTRE project. Fundam Clin Pharmacol. 1997;
11(3):281-284.
49. Horton R, Smith R. Time to register
randomised trials: the case is now unanswerable.
BMJ. 1999;319(7214):865-866.
41. Easterbrook PJ, Berlin JA, Gopalan R, Matthews
DR. Publication bias in clinical research. Lancet.
1991;337(8746):867-872.
50. Dickersin K, Rennie D. The evolution of trial
registries and their use to assess the clinical trial
enterprise. JAMA. 2012;307(17):1861-1864.
42. Stern JM, Simes RJ. Publication bias: evidence
of delayed publication in a cohort study of clinical
research projects. BMJ. 1997;315(7109):640-645.
51. Guyatt GH, Oxman AD, Montori V, et al. GRADE
guidelines, 5: rating the quality of
evidence—publication bias. J Clin Epidemiol. 2011;
64(12):1277-1282.
43. Chan AW, Hróbjartsson A, Haahr MT, Gøtzsche
PC, Altman DG. Empirical evidence for selective
reporting of outcomes in randomized trials:
comparison of protocols to published articles. JAMA.
2004;291(20):2457-2465.
52. Guyatt GH, Oxman AD, Sultan S, et al; GRADE
Working Group. GRADE guidelines, 9: rating up the
quality of evidence. J Clin Epidemiol. 2011;64(12):
1311-1316.
44. Saquib N, Saquib J, Ioannidis JP. Practices and
impact of primary outcome adjustment in
jama.com
JAMA July 9, 2014 Volume 312, Number 2
Copyright 2014 American Medical Association. All rights reserved.
Downloaded From: http://jama.jamanetwork.com/ by a Universidad de Chile User on 10/07/2014
179